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Monotherapy Is Good Enough for Patients with Mild-to-Moderate Alzheimer's Disease: A Network Meta-analysis of 76 Randomized Controlled Trials.
- Source :
-
Clinical pharmacology and therapeutics [Clin Pharmacol Ther] 2019 Jan; Vol. 105 (1), pp. 121-130. Date of Electronic Publication: 2018 Jun 19. - Publication Year :
- 2019
-
Abstract
- Memantine and the Acetylcholinesterase inhibitors (AChEIs) are two classes of drugs that are used to treat patients with Alzheimer's disease. We conducted a network meta-analysis of randomized controlled trials to compare the treatment effectiveness of monotherapy or combination therapy A total of 23,707 AD patients in 76 randomized trials were identified. In patients with mild-to-moderate AD, monotherapy with donepezil, galantamine or rivastigmine were superior to placebo in enhancing cognitive functions and activities of daily living (ADL), whereas monotherapy with donepezil or memantine were superior to placebo in improving behavioral symptoms. However, combination therapy with AChEIs and memantine did not show additional benefit than monotherapy. In patients with moderate-to-severe AD, neither monotherapy nor combination therapy were superior to placebo in any domain measurement. Combination therapy with memantine and AChEIs is confirmed to have no additional benefits over monotherapy. This article is protected by copyright. All rights reserved.<br /> (© 2018 American Society for Clinical Pharmacology and Therapeutics.)
- Subjects :
- Alzheimer Disease diagnosis
Alzheimer Disease epidemiology
Humans
Network Meta-Analysis
Treatment Outcome
Alzheimer Disease drug therapy
Cholinesterase Inhibitors administration & dosage
Dopamine Agents administration & dosage
Memantine administration & dosage
Nootropic Agents administration & dosage
Randomized Controlled Trials as Topic methods
Subjects
Details
- Language :
- English
- ISSN :
- 1532-6535
- Volume :
- 105
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Clinical pharmacology and therapeutics
- Publication Type :
- Academic Journal
- Accession number :
- 29717478
- Full Text :
- https://doi.org/10.1002/cpt.1104